posted on 2020-05-18, 11:35authored byChiara Bruzzone, Ana Loizaga-Iriarte, Pilar Sánchez-Mosquera, Rubén Gil-Redondo, Ianire Astobiza, Tammo Diercks, Ana R. Cortazar, Aitziber Ugalde-Olano, Hartmut Schäfer, Francisco J. Blanco, Miguel Unda, Claire Cannet, Manfred Spraul, José M. Mato, Nieves Embade, Arkaitz Carracedo, Oscar Millet
Prostate
cancer is the second most common tumor and the fifth cause
of cancer-related death among men worldwide. PC cells exhibit profound
signaling and metabolic reprogramming that account for the acquisition
of aggressive features. Although the metabolic understanding of this
disease has increased in recent years, the analysis of such alterations
through noninvasive methodologies in biofluids remains limited. Here,
we used NMR-based metabolomics on a large cohort of urine samples
(more than 650) from PC and benign prostate hyperplasia (BPH) patients
to investigate the molecular basis of this disease. Multivariate analysis
failed to distinguish between the two classes, highlighting the modest
impact of prostate alterations on urine composition and the multifactorial
nature of PC. However, univariate analysis of urine metabolites unveiled
significant changes, discriminating PC from BPH. Metabolites with
altered abundance in urine from PC patients revealed changes in pathways
related to cancer biology, including glycolysis and the urea cycle.
We found out that metabolites from such pathways were diminished in
the urine from PC individuals, strongly supporting the notion that
PC reduces nitrogen and carbon waste in order to maximize their usage
in anabolic processes that support cancer cell growth.